Gene >> DES
| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373960 |
| Start |
219420908:219420908(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.978C>A |
| AA Mutation |
p.His326Gln(p.H326Q) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000373960 |
| Start |
219418749:219418749(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
null
|
| CDS Mutation |
c.287C>T |
| AA Mutation |
p.Ala96Val(p.A96V) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |